meddevicedb.com FDA Device Reference

Simplexa Flu A/B & RSV Direct & Simplexa Flu A/B RSV Positive Control Pack

K142365 Class II Traditional
Decision Date
2014-12-05
Sponsor / Applicant
Focus Diagnostics

Technical Specification

510(k) Submission ID K142365
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2014-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Simplexa Flu A/B & RSV Direct & Simplexa Flu A/B RSV Positive Control Pack received FDA 510(k) clearance under submission number K142365, sponsored by Focus Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2014-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code OCC and 21 CFR 866.3980, within the Microbiology review panel as a Class II device.